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1.南京中医药大学附属医院/江苏省中医院制剂部,南京 210029
2.南京中医药大学药学院,南京 210023
3.江苏省中药资源产业化过程协同创新中心,南京 210023
中药师。研究方向:中药制剂研发与质量控制。 E-mail:zcg0925@163.com
副教授,硕士生导师,博士。研究方向:中药制剂研发与膜分离。E-mail:licunyuok@163.com
收稿日期:2024-11-19,
修回日期:2025-03-09,
录用日期:2025-03-11,
纸质出版日期:2025-05-15
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赵晨光,汤书婉,刘顺,等.指纹图谱结合含量测定分析黄芪闷润和蒸润切制的量值传递规律 [J].中国药房,2025,36(09):1065-1070.
ZHAO Chenguang,TANG Shuwan,LIU Shun,et al.Analysis of the quantity transfer rules in processing of Astragalus membranaceus by moistening-soaking and steaming-soaking followed by cutting based on fingerprint combined with content determination[J].ZHONGGUO YAOFANG,2025,36(09):1065-1070.
赵晨光,汤书婉,刘顺,等.指纹图谱结合含量测定分析黄芪闷润和蒸润切制的量值传递规律 [J].中国药房,2025,36(09):1065-1070. DOI: 10.6039/j.issn.1001-0408.2025.09.08.
ZHAO Chenguang,TANG Shuwan,LIU Shun,et al.Analysis of the quantity transfer rules in processing of Astragalus membranaceus by moistening-soaking and steaming-soaking followed by cutting based on fingerprint combined with content determination[J].ZHONGGUO YAOFANG,2025,36(09):1065-1070. DOI: 10.6039/j.issn.1001-0408.2025.09.08.
目的
2
分析黄芪闷润、蒸润切制前后的量值传递规律。
方法
2
制备3批黄芪闷润、蒸润切制饮片。通过《中药色谱指纹图谱相似度评价系统(2012版)》建立黄芪药材及其闷润、蒸润切制饮片的高效液相色谱叠加指纹图谱,结合前期定性分析结果指认共有峰,分析共有峰峰面积变化,并进行主成分分析。采用高效液相色谱法测定黄芪药材及其闷润、蒸润切制饮片中毛蕊异黄酮苷、黄芪皂苷Ⅰ、黄芪甲苷的含量,并比较不同样品中各成分的含量差异。
结果
2
指纹图谱分析结果显示,共指认了17个共有峰;黄芪闷润、蒸润后,饮片中各共有峰峰面积占比相比药材均发生了变化(如黄芪蒸润切制饮片中丙二酰基毛蕊异黄酮苷和丙二酰基黄芪皂苷Ⅰ峰面积占比降低,毛蕊异黄酮苷峰面积占比升高)。主成分分析结果显示,黄芪药材、黄芪闷润切制饮片、黄芪蒸润切制饮片各自聚为一类。含量测定结果显示,与黄芪药材相比,黄芪闷润切制饮片中毛蕊异黄酮苷的平均含量显著降低(
P
<0.05);黄芪蒸润切制饮片中毛蕊异黄酮苷、黄芪甲苷的平均含量均显著升高(
P
<0.05);黄芪闷润切制饮片中黄芪甲苷以及2种饮片中黄芪皂苷Ⅰ的平均含量差异均无统计学意义(
P
>0.05)。
结论
2
黄芪药材闷润、蒸润切制前后量值传递规律存在差异,其中蒸润切制可能使不稳定成分(如丙二酰基毛蕊异黄酮苷、丙二酰基黄芪皂苷Ⅰ)转化更完全。
OBJECTIVE
2
To analyze the quantity transfer rule in the processing of
Astragalus membranaceus
before and after moistening-soaking and steaming-soaking followed by cutting.
METHODS
2
Three batches of
A. membranaceus
decoction pieces processed through moistening-soaking and steaming-soaking followed by cutting were prepared. The HPLC overlapping fingerprints of
A. membranaceus
and its decoction pieces were established through the
Similarity Evaluation System of Chromatographic Fingerprints of TCM
(
2012 edition
). Combined with the previous qualitative analysis results, the common peaks were identified, the changes of common peak area were analyzed, and the principal component analysis was carried out. The contents of calycosin-7-glucoside, astragaloside Ⅰ and astragaloside Ⅳ in
A. membranaceus
and its dec
oction pieces were determined by HPLC, and the content differences of each component in different samples were compared.
RESULTS
2
The results of fingerprint analysis showed that 17 common peaks were identified. After steaming-soaking and moistening-soaking of
A. membranaceus
, the proportion of common peak area in the decoction pieces changed compared with the original medicine (for example, in
A. membranaceus
steaming-soaking decoction pieces, the proportion of peak area of malonyl calycosin-7-glucoside and malonyl astragaloside Ⅰ decreased, while the proportion of peak area of calycosin-7-glucoside increased). The results of principal component analysis showed that
A. membranaceus
, and its decoction pieces after moistening-soaking and steaming-soaking followed by cutting were all clustered into one category respectively. The results of content determination showed that, compared with
A. membranaceus,
the average content of calycosin-7-glucoside in
A. membranaceus
moistening-soaking decoction pieces was significantly reduced (
P
<0.05); the average contents of calycosin-7-glucoside and astragaloside Ⅳ in
A. membranaceus
steaming-soaking decoction pieces were significantly increased (
P
<0.05); there was no significant difference in the average content of astragaloside Ⅳ in
A. membranaceus
moistening-soaking decoction pieces and astragaloside Ⅰ in the two decoction pieces (
P
>0.05).
CONCLUSIONS
2
There are differences in the quantity transfer rules of
A. membranaceus
before and after moistening-soaking and steaming-soaking followed by cutting. Steaming-soaking followed by cutting may make the transformation of unstable components (such as malonyl calycosin-7-glucoside and malonyl astragaloside Ⅰ) more complete.
国家药典委员会 . 中华人民共和国药典:一部 [M ] . 2020年版 . 北京 : 中国医药科技出版社 , 2020 : 315 .
尚志均 . 雷公炮炙论 [M ] . 合肥 : 安徽科学技术出版社 , 1991 : 37 .
浙江省食品药品监督管理局 . 浙江省中药炮制规范 [M ] . 2015年版 . 北京 : 中国医药科技出版社 , 2015 : 83 .
贵州省食品药品监督管理局 . 贵州省中药饮片炮制规范 [M ] . 2005年版. 贵阳 : 贵州科技出版社 , 2005 : 221 .
上海市药品监督管理局 . 上海市中药饮片炮制规范 [M ] . 2018年版 . 上海 : 上海科学技术出版社 , 2018 : 150 .
江苏省药品监督管理局 . 江苏省中药饮片炮制规范 [M ] . 2002年版. 南京 : 江苏科学技术出版社 , 2002 : 114 .
刘蓬蓬 , 史辑 , 张凡 , 等 . UPLC同时测定4种酶定向炮制黄芪中的6种黄酮类成分含量 [J ] . 中国实验方剂学杂志 , 2020 , 26 ( 10 ): 94 - 99 .
CHUANKHAYAN P , RIMLUMDUAN T , SVASTI J , et al . Hydrolysis of soybean isoflavonoid glycosides by Dalbergia β-glucosidases [J ] . J Agric Food Chem , 2007 , 55 ( 6 ): 2407 - 2412 .
孙乐 , 吴鹏 , 王春艳 , 等 . 黄芪饮片炮制工艺优选 [J ] . 时珍国医国药 , 2020 , 31 ( 7 ): 1616 - 1619 .
陈淑珍 , 孙恬 , 谭丽容 , 等 . 黄芪切片中黄芪甲苷含量变化研究 [J ] . 安徽农业科学 , 2021 , 49 ( 9 ): 166 - 167,171 .
余书琦 , 李志强 , 赵宇菁 . 不同切制工艺对黄芪有效成分含量的影响 [J ] . 时珍国医国药 , 2017 , 28 ( 8 ): 1886 - 1888 .
国家药典委员会 . 中华人民共和国药典:四部 [M ] . 2020年版 . 北京 : 中国医药科技出版社 , 2020 : 683 .
赵晨光 , 李存玉 , 杨珊 , 等 . 基于道地产区蒙古黄芪的质量差异性分析 [J ] . 中国中药杂志 , 2020 , 45 ( 13 ): 3183 - 3190 .
ZHENG Y F , DUAN W P , SUN J , et al . Structural identification and conversion analysis of malonyl isoflavonoid glycosides in Astragali Radix by HPLC coupled with ESI-Q TOF/MS [J ] . Molecules , 2019 , 24 ( 21 ): 3929 .
CHU C , CAI H X , REN M T , et al . Characterization of novel astragaloside malonates from Radix Astragali by HPLC with ESI quadrupole TOF MS [J ] . J Sep Sci , 2010 , 33 ( 4/5 ): 570 - 581 .
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